A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003285



Internal ID18745817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31386933..33172886hg38UCSC Ensembl
Innerchr3:31428425..33214378hg19UCSC Ensembl
Innerchr3:31403429..33189382hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381785954
hg191785954
hg181785954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589582
Samples
Known GenesCCR4, CMTM6, CMTM7, CMTM8, CNOT10, CRTAP, DYNC1LI1, GLB1, GPD1L, OSBPL10, OSBPL10-AS1, STT3B, SUSD5, TMPPE, TRIM71, ZNF860
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003285
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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